510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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MIHClass III

System, Endovascular Graft, Aortic Aneurysm Treatment

Unknown
FDA source (opens on fda.gov)

MIH is the FDA product code for System, Endovascular Graft, Aortic Aneurysm Treatment, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 176 recalls.

Classification record

Product code
MIH
Device name
System, Endovascular Graft, Aortic Aneurysm Treatment
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
176

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 27 companies shown, in name order